Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 beta gene.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Sept 2010

Giglio Sabrina, Contini Elisa, Toni Sonia, Pela Ivana

Abstract excerpt

We provide a molecular and pathophysiological characterization of an 11-year-old male patient, with a diagnosis of renal hypodysplasia, cysts and chronic renal failure. Although previously normoglycaemic and with a negative familial history for diabetes mellitus, he developed fasting hyperglycaemia within 12 months of the start of treatment with recombinant human growth hormone (rhGH). Direct sequencing of the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child
Share to Hepatocyte Nuclear Factor 1-beta

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Human Growth Hormone

Share to Hyperglycemia

Share to Kidney Diseases, Cystic

Share to Kidney Failure, Chronic

Share to Prognosis

Share to Recombinant Proteins

Source

Identifiers

PMID: 20543213
DOI: 10.1093/ndt/gfq315

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 beta gene.PMID 20543213Read ↗

New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation.Semantic proximity Read ↗

Mutations in hepatocyte nuclear factor-1β and their related phenotypesSemantic proximity Read ↗

HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.Semantic proximity Read ↗

Case Report: A Multisystem Mystery: Unraveling HNF1β-Associated Glomerulocystic Disease in a 30-year-old FemaleSemantic proximity Read ↗

A Novel Mutation of the HNF1B Gene Associated With Hypoplastic Glomerulocystic Kidney Disease and Neonatal Renal FailureSemantic proximity Read ↗

Severe pancreas hypoplasia and multicystic renal dysplasia in two human fetuses carrying novel HNF1β/MODY5 mutationsSemantic proximity Read ↗

Heterozygous recurrent HNF4A variant p.Arg85Trp causes Fanconi renotubular syndrome 4 with maturity onset diabetes of the young, an autosomal dominant phenocopy of Fanconi Bickel syndrome with colobomas.Semantic proximity Read ↗

Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1Semantic proximity Read ↗

A complex microdeletion 17q12 phenotype in a patient with recurrent de novo membranous nephropathy.Semantic proximity Read ↗

Hepatocyte nuclear factor-1 gene deletions--a common cause of renal diseaseSemantic proximity Read ↗

Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease.Semantic proximity Read ↗

Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.